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Heather A. Whitlaw

Publications and source records attributed to Heather A. Whitlaw.

9 recordsLinked to original sources
USGS2017

Nesting ecology of grassland birds following a wildfire in the southern Great Plains

We studied the response of nesting grassland birds occupying short-grass and mixed-grass prairie sites 2 and 3 y following two, large-scale wildfires that burned ≥360,000 ha in the Texas Panhandle in March 2006. Nest success was greater on burned plots compared to unburned plots, though this varied by species and year. Woody vegetation cover was greater around nests on unburned plots compared to burned plots for Cassin's sparrow ( Peucaea cassinii ) and lark sparrow ( Chondestes grammacus ). Cassin's sparrows and lark sparrows nested in more-woody vegetation than did grasshopper sparrows ( Ammodramus savannarum ), and woody vegetation was reduced following the wildfires. The wildfires appear to have had few if any negative influences on the avian community 3 years postfire. This may be due to grassland breeding birds being adapted to landscapes in which, historically, periodic disturbance (e.g., wildfire, intensive grazing by bison [ Bison bison ]) resulted in vegetation heterogeneity.

Texas↗
USGS2013

Spatially explicit modeling of lesser prairie-chicken lek density in Texas

As with many other grassland birds, lesser prairie-chickens (Tympanuchus pallidicinctus) have experienced population declines in the Southern Great Plains. Currently they are proposed for federal protection under the Endangered Species Act. In addition to a history of land-uses that have resulted in habitat loss, lesser prairie-chickens now face a new potential disturbance from energy development. We estimated lek density in the occupied lesser prairie-chicken range of Texas, USA, and modeled anthropogenic and vegetative landscape features associated with lek density. We used an aerial line-transect survey method to count lesser prairie-chicken leks in spring 2010 and 2011 and surveyed 208 randomly selected 51.84-km(2) blocks. We divided each survey block into 12.96-km(2) quadrats and summarized landscape variables within each quadrat. We then used hierarchical distance-sampling models to examine the relationship between lek density and anthropogenic and vegetative landscape features and predict how lek density may change in response to changes on the landscape, such as an increase in energy development. Our best models indicated lek density was related to percent grassland, region (i.e., the northeast or southwest region of the Texas Panhandle), total percentage of grassland and shrubland, paved road density, and active oil and gas well density. Predicted lek density peaked at 0.39leks/12.96km(2) (SE=0.09) and 2.05leks/12.96km(2) (SE=0.56) in the northeast and southwest region of the Texas Panhandle, respectively, which corresponds to approximately 88% and 44% grassland in the northeast and southwest region. Lek density increased with an increase in total percentage of grassland and shrubland and was greatest in areas with lower densities of paved roads and lower densities of active oil and gas wells. We used the 2 most competitive models to predict lek abundance and estimated 236 leks (CV=0.138, 95% CI=177-306leks) for our sampling area. Our results suggest that managing landscapes to maintain a greater percentage of grassland and shrubland on the landscape with a greater ratio of grasses to shrubs in the northeast Panhandle should promote greater lek density. Furthermore, increases in paved road and active oil and gas well densities may reduce lek density. This information will be useful for future conservation planning efforts for land protection, policy decisions, and decision analyses.

Journal of Wildlife Management↗
USGS2013

Abundance and density of lesser prairie-chickens and leks in Texas

Lesser prairie-chickens (LEPCs; Tympanuchus pallidicinctus) have experienced population declines due to both direct and indirect habitat loss, including conversion of native rangeland to cropland and disturbance from energy development. Our objectives were to 1) determine the current density of LEPC leks and LEPCs within the Texas (USA) occupied range, including areas with high potential for wind-energy development; and 2) find new leks. To estimate lek and LEPC density, we employed a line-transect-based aerial survey method using a Robinson 22 helicopter to count leks. We surveyed 26,810.9 km of transect in the spring of 2010 and 2011 and we detected 96 leks. We estimated a density of 2.0 leks/100 km(2) (90% CI = 1.4-2.7 leks/100 km(2)) and 12.3 LEPCs/100 km(2) (90% CI = 8.5-17.9 LEPCs/100 km(2)) and an abundance of 293.6 leks (90% CI = 213.9-403.0 leks) and 1,822.4 LEPCs (90% CI = 1,253.7-2,649.1 LEPCs) for our sampling frame. Our best model indicated that lek size and lek type (AIC(c) wt = 0.235) influenced lek detectability. Lek detectability was greater for larger leks and natural leks versus man-made leks. Our statewide survey efforts provide wildlife managers and biologists with population estimates, new lek locations, and areas to target for monitoring and conservation.

Wildlife Society Bulletin↗
USGS2012

Raptor community composition in the Texas Southern High Plains lesser prairie-chicken range

Predation can be a factor in preventing prey population growth and sustainability when prey populations are small and fragmented, and when predator density is unrelated to the density of the single prey species. We conducted monthly raptor surveys from February 2007 to May 2009 in adjacent areas of the Texas Southern High Plains (USA) that do and do not support lesser prairie-chickens ( Tympanuchus pallidicinctus ), a candidate for protection under the Endangered Species Act. During the summer period corresponding to prairie-chicken nesting and brood-rearing, Swainson's hawks ( Buteo swainsoni ) were the most abundant raptor. During the lekking and overwintering period, the raptor community was diverse, with northern harriers ( Circus cyaneus ) being the most abundant species. Raptor abundance peaked during the early autumn and was lowest during the spring. Utility poles were a significant predictor of raptor density at survey points and Swainson's hawks and all raptors, pooled, were found in greater densities in non-prairie-chicken habitat dominated by mesquite ( Prosopis glandulosa ). Avian predation risk on prairie-chickens, based on presence and abundance of raptors, appears to be greatest during winter when there is a more abundant and diverse raptor community, and in areas with utility poles.

Wildlife Society Bulletin↗
USGS2012

Grassland bird communtiy response to large wildfires

We studied breeding season communities of grassland birds on short-grass and mixed-grass prairie sites during the second and third breeding seasons following two large wildfires in March 2006 in the Texas panhandle, USA. There was an apparent temporary shift in avian community composition following the fires due to species-specific shifts associated with life-history traits and vegetation preferences. Species that prefer sparse vegetation and bare ground on short-grass sites, such as Horned Lark ( Eremophila alpestris ), benefited from wildfires, while others, such as Western Meadowlark ( Sturnella neglecta ), that prefer more dense vegetation, were negatively impacted. Mixed-grass sites had species-specific shifts in 2007, two breeding seasons after the fires; grassland bird communities on burned plots were similar by 2008 to those on unburned plots. Avian communities appeared to return to pre-burn levels within 3 years following wildfires. Many of the responses in our study of wildfire were similar to those reported following prescribed fires elsewhere. Prescribed fires appear to have similar effects on the avian community despite differences in intensity and environmental conditions during wildfires.

Wilson Journal of Ornithology↗
USGS2012

Sexual selection and mating chronology of Lesser Prairie-Chickens

Little is known about mate selection and lek dynamics of Lesser Prairie-Chickens (Tympanuchus pallidicinctus). We collected data on male territory size and location on leks, behavior, and morphological characteristics and assessed the importance of these variables on male Lesser Prairie-Chicken mating success during spring 2008 and 2009 in the Texas Southern High Plains. We used discrete choice models and found that males that were less idle were chosen more often for mating. Our results also suggest that males with smaller territories obtained more copulations. Morphological characteristics were weaker predictors of male mating success. Peak female attendance at leks occurred during the 1-week interval starting 13 April during both years of study. Male prairie-chickens appear to make exploratory movements to, and from, leks early in the lekking season; 13 of 19 males banded early (23 Feb–13 Mar) in the lekking season departed the lek of capture and were not reobserved (11 yearlings, 2 adults). Thirty-three percent (range = 26–51%) of males on a lek mated (yearlings = 44%, adults = 20%) and males that were more active experienced greater mating success.

Wilson Journal of Ornithology↗
USGS2011

Interactions of raptors and Lesser Prairie-Chickens at leks in the Texas Southern High Plains

We examined behavioral interactions of raptors, Chihuahuan Ravens ( Corvus cryptoleucus ), and Lesser Prairie-Chickens ( Tympanuchus pallidicinctus ) at leks in the Texas Southern High Plains. Northern Harriers ( Circus cyaneus ) and Swainson's Hawks ( Buteo swainsoni ) were the most common raptors observed at leks. Only 15 of 61 (25%) raptor encounters at leks (0.09/hr) resulted in a capture attempt (0.02/hr). Mean (± SD) time for Lesser Prairie-Chickens to return to lekking behavior following a raptor encounter was 4.2 ± 5.5 min suggesting the disturbance had little influence on lekking behaviors. Lesser Prairie-Chickens engaged in different escape behaviors depending on raptor species and, generally, did not respond to ravens suggesting they are able to assess different predation risks. The raptors in our study area posed little predation risk to lekking prairie-chickens. Behavioral disturbance at leks appears minimal due to the lack of successful predation events, low raptor encounter rates, and short time to return to lekking behavior.

Texas↗
USGS2006

Pathogens, nutritional deficiency, and climate influences on a declining moose population

Several potential proximate causes may be implicated in a recent (post-1984) decline in moose ( Alces alces andersoni ) numbers at their southern range periphery in northwest Minnesota, USA. These causes include deleterious effects of infectious pathogens, some of which are associated with white-tailed deer ( Odocoileus virginianus ), negative effects of climate change, increased food competition with deer or moose, legal or illegal hunting, and increased predation by gray wolves ( Canis lupus ) and black bears ( Ursus americanus ). Long-standing factors that may have contributed to the moose decline include those typically associated with marginal habitat such as nutritional deficiencies. We examined survival and productivity among radiocollared ( n = 152) adult female and juvenile moose in northwest Minnesota during 1995–2000, and assessed cause of death and pathology through carcass necropsy of radiocollared and non-radiocollared animals. Aerial moose surveys suggested that hunting was an unlikely source of the numerical decline because the level of harvest was relatively low (i.e., approx. 15% / 2 yr) and the population usually grew in years following a hunt. The majority of moose mortalities (up to 87% of radiocollared moose [ n = 76] and up to 65% of non-radiocollared moose [ n = 84]) were proximally related to pathology associated with parasites and infectious disease. Liver fluke ( Fascioloides magna ) infections apparently constituted the greatest single source of mortality and caused significant pathology in the liver, thoracic and peritoneal cavities, pericardial sac, and lungs. Mortality due to meningeal worm ( Parelaphostrongylus tenuis ) was less prevalent and was manifested through characteristic neurological disease. Several mortalities apparently were associated with unidentified infectious disease, probably acting in close association with malnutrition. Bone-marrow fat was lower for moose dying of natural causes than those dying of anthropogenic factors or accidents, implying that acute malnutrition contributed to moose mortality. Blood profiles from live-captured animals indicated that those dying in the subsequent 18 months were chronically malnourished. Relative to other populations, average annual survival rates for adult females (0.79 [0.74–0.84; 95% CI]) and yearlings (0.64 [0.48–0.86]) were low, whereas those for calves (0.66 [0.53–081]) were high. Pregnancy (48%) and twinning (19%) rates were among the lowest reported for moose, with reproductive senescence among females being apparent as early as 8 years. Pregnancy status was related to indices of acute (i.e., bone-marrow fat) and chronic (i.e., blood condition indices) malnutrition. Opportunistic carcass recovery indicated that there likely were few prime-aged males (>5 yr old) in the population. Analysis of protein content in moose browse and fecal samples indicated that food quality was probably adequate to support moose over winter, but the higher fecal protein among animals that died in the subsequent 18 months could be indicative of protein catabolism associated with malnutrition. Trace element analysis from moose livers revealed apparent deficiencies in copper and selenium, but there was limited evidence of direct association between trace element concentrations and moose disease, pathology, or mortality. Time-series analysis of regional moose counts (1961–2000) indicated that annual population growth rate was related negatively to mean summer temperature, with winter and summer temperatures increasing by an average of 6.8 and 2.1 C, respectively, during the 40-year period. This change may have increased moose thermoregulatory costs and disrupted their energy balance, and thereby reduced their fitness. Time-series analysis failed to show a relationship between annual population growth rate and moose or deer abundance, indicating that food limitation via resource competition was unlikely. Population viability analyses, using count data (1961–2000) and demographic data collected during this study, suggested that the northwest Minnesota moose population likely would not persist over the next 50 years. More broadly, we conclude that the southern distribution of moose may become restricted in areas where climate and habitat conditions are marginal, especially where deer are abundant and act as reservoir hosts for parasites.

Minnesota↗